๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

A Novel Germline Mutation in the von Hippel-Lindau Gene in Patients in Kuwait

โœ Scribed by AlFadhli, Suad; Salim, Matra; Al-Awadi, Sadiqa


Book ID
115452406
Publisher
S. Karger AG
Year
2004
Tongue
English
Weight
168 KB
Volume
13
Category
Article
ISSN
1011-7571

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Improved detection of germline mutations
โœ Catherine Stolle; Gladys Glenn; Berton Zbar; Jeffrey S. Humphrey; Peter Choyke; ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 201 KB ๐Ÿ‘ 2 views

Communicated by Victor A. McKusick von Hippel-Lindau disease (VHL) is an inherited neoplastic disorder characterized by the development of tumors in the eyes, brain, spinal cord, inner ear, adrenal gland, pancreas, kidney, and epididymis. The VHL tumor suppressor gene was identified in 1993. Initial

Germline mutation profile of the VHL gen
โœ Sylviane Olschwang; Stรฉphane Richard; Cรฉcile Boisson; Sophie Giraud; Pierre Laur ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 252 KB ๐Ÿ‘ 2 views

## Communicated by Lap-Chee Tsui Von Hippel-Lindau (VHL) disease is a dominantly inherited disorder predisposing those afflicted to hemangioblastomas of the central nervous system and the retina, renal cell carcinomas, pheochromocytomas, and pancreatic tumors. The disease has been associated with